List of 5α-reductase inhibitors
This is a list of 5α-reductase inhibitors (5α-RIs), drugs which inhibit one or more isoforms of the enzyme 5α-reductase. This enzyme is responsible for the conversion of the androgen hormone testosterone into the more potent dihydrotestosterone (DHT) and is essential for the production of neurosteroids like allopregnanolone, tetrahydrodeoxycorticosterone (THDOC), and 3α-androstanediol from progesterone, deoxycorticosterone, and DHT, respectively. 5α-Reductase inhibitors have medical applications in the treatment of benign prostatic hyperplasia, androgenic alopecia (pattern hair loss), and hirsutism (excessive hair growth).
Pharmaceutical drugs
5α-RIs used in medicine include the following:
- Finasteride (Proscar, Propecia)
- Dutasteride (Avodart)
- Epristeride (Aipuliete, Chuanliu)
- Alfatradiol (Ell-Cranell Alpha, Pantostin)
- Saw palmetto extract (Permixon)
Research drugs
Some of the 5α-RIs in research are as follows:
- Bexlosteride (LY-191704)
- Izonsteride (LY-320236)
- Lapisteride (CS-891)
- Turosteride (FCE-26073)
- FCE-28260
- MK-386 (L-733692)
- PNU 157706[1]
- LY 266111
- EM-402
- AS 97004
- FK 143
- ONO-3805
- Z-350[2]
- L-751788 16-((4-chlorophenyl)oxy)-4,7-dimethyl-4-azaandronstan-3-one
- 4-MA (Dual inhibitor of both I & II isozymes (IC50 = 8.5 nM), but also 3-β-HSD inhibitor, investigated extensively but said to be hepatotoxic).[3]
- MK-434 (17 beta-benzoyl-4-aza-5 alpha-androst-1-ene-3-one).[4]
- MK-963 (L-654066)
- FR146687 and FK143 (Fujisawa Pharmaceutical) {Indolizine- and Indol-Butanoic Acids}
- 17β-carboxy-4-androsten-3-one {[5] in [6]}
- Steroidal oxime[7][8]
Herbs and other inhibitors
Many plants, as well as their associated phytochemical constituents, have inhibitory effects on 5α-reductase.[9] In addition, many of these compounds are also phytoestrogens.[10] Examples include the following:
- Zinc.[11]
- Riboflavin (vitamin B2).[12]
- Azelaic acid,[11] (sometimes combined with minoxidil hair solution).
- β-Sitosterol,[13] is just one of the many phytosterols.
- Polyphenols[14]
- Alizarin,
- Curcumin, the principal curcuminoid of turmeric.
- Green tea catechins, including (-)-epicatechin-3-gallate, and (-)-epigallo-catechin-3-gallate (EGCG).[15]
- Valoneic acid dilactone and gallagyldilactone are two hydrolysable tannin polyphenols isolated from the heartwood of Shorea laeviforia[16] and oaks species such as the North American white oak (Quercus alba) and European red oak (Quercus robur) are inhibitory.[17]
- Angelica koreana [18][19]
- Garden Balsam or Rose Balsam (Impatiens balsamina)[20]
- Pollen of Turnip, turnip rape, fast plants, field mustard, or turnip mustard (Brassica rapa)[21]
- Dodder (Cuscuta reflexa)[22]
- Euphorbia jolkinii[23][24]
- Lingzhi mushroom or Reishi mushroom (Ganoderma lucidum)[25][26][27][28]
- Ganoderic acid,[29] or Ganoderol B are thought to be the compounds in the mushroom that are specifically active.[30]
- Chinese Knotweed (Polygonum multiflorum),[31] contains resveratrol-like Stilbenoids.
- Black Pepper leaf extract (Piper nigrum) [32]
- Red Stinkwood (Pygeum africanum)[33]
- Saw Palmetto (Serenoa repens, active substance possibly lauric acid[34])[35][36]
- The berries of saw palmetto (Serenoa repens), a small palm native to the south east United States, possess a dual 5a-reductase inhibition activity, due to their high content of phytosterols: β-sitosterol, stigmasterol, lupeol, lupenone, and cycloartenol. Permixon® was launched in Europe in 1984 but has no FDA approval. The lipido-sterol extract markedly inhibits both the human isoenzymes. Type 1 isoenzyme is noncompetitively (Ki = 7.2 μg/mL) and type 2 isoenzyme uncompetitively (Ki = 4.9 μg/mL) inhibited[37]
- Pine (Pinus sp. resin, active substance abietic acid)[38]
- Ku Shen or Bitter root (Sophora flavescens)[39]
- Japanese hedge parsley (Torilis japonica)[40]
- Eastern Arborvitae, Northern Whitecedar (Thuja occidentalis)[41]
- Spore of Japanese climbing fern (Lygodium japonicum)[42]
- The relative inhibitory potencies of unsaturated fatty acids are, in decreasing order: Gamma-Linolenic acid, alpha-linolenic acid, linoleic acid, palmitoleic acid, oleic acid, and myristoleic acid.[43]
- Medium chain fatty acids such as those found in coconut and the kernel of many palm fruits have also been found to inhibit 5α-reductase.[44]
- Certain pesticides are able to disturb the sex steroid hormone system and to act as antiandrogens.[45]
These supplements have limited testing in human clinical trials, and their potential for the treatment of BPH, androgenic alopecia, and related conditions is unknown.
References
- ↑ Di Salle, E.; Giudici, D.; Radice, A.; Zaccheo, T.; Ornati, G.; Nesi, M.; Panzeri, A.; Délos, S.; Martin, P. M. (1998). "PNU 157706, a novel dual type I and II5α-reductase inhibitor". The Journal of Steroid Biochemistry and Molecular Biology. 64 (3–4): 179–86. PMID 9605412. doi:10.1016/S0960-0760(97)00158-1.
- ↑ http://jpet.aspetjournals.org/content/290/3/1013.full.pdf
- ↑ Guarna, A.; Occhiato, E.; Danza, G.; Conti, A.; Serio, M. (1998). "5α-Reductase Inhibitors, Chemical and Clinical Models". Steroids. 63 (5–6): 355–61. PMID 9618802. doi:10.1016/S0039-128X(98)00020-8.
- ↑ Cohen, S. M.; Werrmann, J. G.; Rasmusson, G. H.; Tanaka, W. K.; Malatesta, P. F.; Prahalada, S; Jacobs, J. G.; Harris, G; Nett, T. M. (1995). "Comparison of the effects of new specific azasteroid inhibitors of steroid 5 alpha-reductase on canine hyperplastic prostate: Suppression of prostatic DHT correlated with prostate regression". The Prostate. 26 (2): 55–71. PMID 7531846. doi:10.1002/pros.2990260202.
- ↑ Hsia, S. L.; Voigt, W. (1974). "Inhibition of Dihydrotestosterone Formation: An Effective Means of Blocking Androgen Action in Hamster Sebaceous Gland". Journal of Investigative Dermatology. 62 (3): 224–7. PMID 4361987. doi:10.1111/1523-1747.ep12676791.
- ↑ "Steroid 5α α α α-Reductase Inhibitors" (PDF). ResearchGate. 2014-05-21. Retrieved 2014-06-08.
- ↑ Hartmann, R. W.; Hector, M.; Haidar, S.; Ehmer, P. B.; Reichert, W.; Jose, J. (2000). "Synthesis and Evaluation of Novel Steroidal Oxime Inhibitors of P450 17 (17α-Hydroxylase/C17−20-Lyase) and 5α-Reductase Types 1 and 2". Journal of Medicinal Chemistry. 43 (22): 4266–77. PMID 11063622. doi:10.1021/jm001008m.
- ↑ Flores, E; Bratoeff, E; Cabeza, M; Ramirez, E; Quiroz, A; Heuze, I (2003). "Steroid 5alpha-reductase inhibitors". Mini reviews in medicinal chemistry. 3 (3): 225–37. PMID 12570838. doi:10.2174/1389557033488196.
- ↑ "Evaluation of 5α-reductase inhibitory activity of certain herbs useful as antiandrogens.". ResearchGate. Retrieved 2014-06-08.
- ↑ http://www.botanicalmedicine.org/References/09merefs/StansburyPhytoestRef.pdf
- 1 2 Stamatiadis D, Bulteau-Portois MC, Mowszowicz I (November 1988). "Inhibition of 5 alpha-reductase activity in human skin by zinc and azelaic acid". The British Journal of Dermatology. 119 (5): 627–32. PMID 3207614. doi:10.1111/j.1365-2133.1988.tb03474.x.
- ↑ "RIBOFLAVIN, A TESTOSTERONE 5α-REDUCTASE INHIBITOR". Jstage.jst.go.jp. doi:10.7164/antibiotics.43.1615. Retrieved 2014-06-08.
- ↑ Cabeza M, Bratoeff E, Heuze I, Ramírez E, Sánchez M, Flores E (2003). "Effect of beta-sitosterol as inhibitor of 5 alpha-reductase in hamster prostate". Proceedings of the Western Pharmacology Society. 46: 153–5. PMID 14699915.
- ↑ Hiipakka RA, Zhang HZ, Dai W, Dai Q, Liao S (March 2002). "Structure-activity relationships for inhibition of human 5alpha-reductases by polyphenols". Biochemical Pharmacology. 63 (6): 1165–76. doi:10.1016/s0006-2952(02)00848-1.
- ↑ Liao, S.; Lin, J.; Dang, M. T.; Zhang, H.; Kao, Y. H.; Fukuchi, J.; Hiipakka, R. A. (2001). "Growth suppression of hamster flank organs by topical application of catechins, alizarin, curcumin, and myristoleic acid". Archives of dermatological research. 293 (4): 200–205. PMID 11380153. doi:10.1007/s004030000203.
- ↑ Hirano Yoshio; Kondo Ryuichiro; Sakai Kokki. "5A-Reductase inhibitory tannin-related compounds isolated from Shorea laeviforia". Journal of wood science. 49 (4): 339–343. doi:10.1007/s10086-002-0481-y.
- ↑ Mämmelä Pirjo; Savolainenb Heikki; Lindroosa Lasse; Kangasd Juhani; Vartiainen Terttu (2000). "Analysis of oak tannins by liquid chromatography-electrospray ionisation mass spectrometry". Journal of Chromatography A. 891 (1): 75–83. PMID 10999626. doi:10.1016/S0021-9673(00)00624-5.
- ↑ Plants for a Future: Angelica koreana
- ↑ Seo, EK; Kim, KH; Kim, MK; Cho, MH; Choi, E; Kim, K; Mar, W (2002). "Inhibitors of 5alpha -reductase type I in LNCaP cells from the roots of Angelica koreana.". Planta Medica. 68 (2): 162–3. PMID 11859469. doi:10.1055/s-2002-20258.
- ↑ Oku H. Ishiguro K. (2002). "Cyclooxygenase-2 inhibitory 1,4-naphthoquinones from Impatiens balsamina L.". Biological & Pharmaceutical Bulletin. 25 (5): 658–60. doi:10.1248/bpb.25.658.
- ↑ Li, YH; Yang, YF; Li, K; Jin, LL; Yang, NY; Kong, DY (2009). "5 alpha-reductase and aromatase inhibitory constituents from Brassica rapa L. pollen.". Chemical & pharmaceutical bulletin. 57 (4): 401–4. PMID 19336936. doi:10.1248/cpb.57.401.
- ↑ Pandit S. Chauhan NS. Dixit VK (2008). "Effect of Cuscuta reflexa Roxb on androgen-induced alopecia". Journal of Cosmetic Dermatology. 7 (3): 199–204. PMID 18789055. doi:10.1111/j.1473-2165.2008.00389.x.
- ↑ Flora of China: Euphorbia jolkinii
- ↑ Park, SH; Kim, JA; Hua, XG (2005). "Isolation of 5α-reductase inhibitors from Euphorbia jolkinii". Korean Journal of Pharmacognosy. 36 (1): 9–16.
- ↑ Fujita R. Liu J. Shimizu K. Konishi F. Noda K. Kumamoto S. Ueda C. Tajiri H. Kaneko S. Suimi Y. Kondo R."Anti-androgenic activities of Ganoderma lucidum.", Journal of Ethnopharmacology. 102(1):107-12, 2005 Oct 31.
- ↑ Liu J, Kurashiki K, Shimizu K, Kondo R (February 2006). "5alpha-reductase inhibitory effect of triterpenoids isolated from Ganoderma lucidum". Biol. Pharm. Bull. 29 (2): 392–5. PMID 16462054. doi:10.1248/bpb.29.392.
- ↑ Liu, J; Tamura, S; Kurashiki, K; Shimizu, K; Noda, K; Konishi, F; Kumamoto, S; Kondo, R (2009). "Anti-androgen effects of extracts and compounds from Ganoderma lucidum.". Chemistry & Biodiversity. 6 (2): 231–43. PMID 19235153. doi:10.1002/cbdv.200800019.
- ↑ Noguchi, M; Kakuma, T; Tomiyasu, K; Yamada, A; Itoh, K; Konishi, F; Kumamoto, S; Shimizu, K; Kondo, R; Matsuoka, Kei (2008). "Randomized clinical trial of an ethanol extract of Ganoderma lucidum in men with lower urinary tract symptoms.". Asian Journal of Andrology. 10 (5): 777–85. PMID 18097505. doi:10.1111/j.1745-7262.2008.00361.x.
- ↑ Liu, J; Shiono, J; Shimizu, K; Kukita, A; Kukita, T; Kondo, R (2009). "Ganoderic acid DM: anti-androgenic osteoclastogenesis inhibitor.". Bioorganic & Medicinal Chemistry Letters. 19 (8): 2154–7. PMID 19289282. doi:10.1016/j.bmcl.2009.02.119.
- ↑ Liu, J; Shimizu, K; Konishi, F; Kumamoto, S; Kondo, R (2007). "The anti-androgen effect of ganoderol B isolated from the fruiting body of Ganoderma lucidum.". Bioorganic & Medicinal Chemistry. 15 (14): 4966–72. PMID 17499997. doi:10.1016/j.bmc.2007.04.036.
- ↑ Cho, CH; Bae, JS; Kim, YU (2010). "5alpha-reductase inhibitory components as antiandrogens from herbal medicine.". Journal of acupuncture and meridian studies. 3 (2): 116–8. PMID 20633525. doi:10.1016/S2005-2901(10)60021-0.
- ↑ Hirata, N; Tokunaga, M; Naruto, S; Iinuma, M; Matsuda, H (2007). "Testosterone 5alpha-reductase inhibitory active constituents of Piper nigrum leaf.". Biological & Pharmaceutical Bulletin. 30 (12): 2402–5. PMID 18057734. doi:10.1248/bpb.30.2402.
- ↑ Edgar AD. Levin R. Constantinou CE. Denis L. "A critical review of the pharmacology of the plant extract of Pygeum africanum in the treatment of LUTS.Neurourology & Urodynamics. 26(4):458-63; discussion 464, 2007" [Review]
- ↑ Raynaud, JP; Cousse, H; Martin, PM (2002). "Inhibition of type 1 and type 2 5alpha-reductase activity by free fatty acids, active ingredients of Permixon". The Journal of Steroid Biochemistry and Molecular Biology. 82 (2–3): 233–9. PMID 12477490. doi:10.1016/S0960-0760(02)00187-5.
- ↑ Pais, P (2010). "Potency of a novel saw palmetto ethanol extract, SPET-085, for inhibition of 5alpha-reductase II.". Advances in therapy. 27 (8): 555–63. PMID 20623347. doi:10.1007/s12325-010-0041-6.
- ↑ Abe, M; Ito, Y; Oyunzul, L; Oki-Fujino, T; Yamada, S (2009). "Pharmacologically relevant receptor binding characteristics and 5alpha-reductase inhibitory activity of free Fatty acids contained in saw palmetto extract.". Biological & Pharmaceutical Bulletin. 32 (4): 646–50. PMID 19336899. doi:10.1248/bpb.32.646.
- ↑ Iehlé, C.; Délos, S.; Guirou, O.; Tate, R.; Raynaud, J. P.; Martin, P. M. (1995). "Human prostatic steroid 5α-reductase isoforms—A comparative study of selective inhibitors". The Journal of Steroid Biochemistry and Molecular Biology. 54 (5–6): 273–9. PMID 7577710. doi:10.1016/0960-0760(95)00134-L.
- ↑ Roh, SS; Park, MK; Kim, YU (2010). "Abietic acid from Resina Pini of Pinus species as a testosterone 5α-reductase inhibitor". Journal of Health Science. 56 (4): 451–455. doi:10.1248/jhs.56.451.
- ↑ Roh, SS; Kim, CD; Lee, MH; Hwang, SL; Rang, MJ; Yoon, YK (2002). "The hair growth promoting effect of Sophora flavescens extract and its molecular regulation.". Journal of dermatological science. 30 (1): 43–9. PMID 12354419. doi:10.1016/s0923-1811(02)00060-9.
- ↑ Park, WS; Son, ED; Nam, GW; Kim, SH; Noh, MS; Lee, BG; Jang, IS; Kim, SE; Lee, JJ; Lee, CH (2003). "Torilin from Torilis japonica, as a new inhibitor of testosterone 5 alpha-reductase.". Planta Medica. 69 (5): 459–61. PMID 12802730. doi:10.1055/s-2003-39717.
- ↑ Park, WS; Lee, CH; Lee, BG; Chang, IS (2003). "The extract of Thujae occidentalis semen inhibited 5alpha-reductase and androchronogenetic alopecia of B6CBAF1/j hybrid mouse.". Journal of dermatological science. 31 (2): 91–8. PMID 12670719. doi:10.1016/s0923-1811(02)00146-9.
- ↑ Matsuda H., Yamazaki M., Naruto S., Asanuma Y., Kubo M. "Anti-androgenic and hair growth promoting activities of Lygodii Spora (spore of Lygodium japonicum) I. Active constituents inhibiting testosterone 5α-reductase " Biological and Pharmaceutical Bulletin 2002 25:5 (622-626)
- ↑ Liang, T.; Liao, S. (1992). "Inhibition of steroid 5 alpha-reductase by specific aliphatic unsaturated fatty acids". The Biochemical Journal. 285 (Pt 2): 557–562. PMC 1132824 . PMID 1637346. doi:10.1042/bj2850557.
- ↑ Liu, J; Shimizu, K; Kondo, R (2009). "Anti-androgenic activity of fatty acids.". Chemistry & Biodiversity. 6 (4): 503–12. PMID 19353546. doi:10.1002/cbdv.200800125.
- ↑ Lo, S; King, I; Alléra, A; Klingmüller, D (2007). "Effects of various pesticides on human 5alpha-reductase activity in prostate and LNCaP cells.". Toxicology in Vitro. 21 (3): 502–8. PMID 17218080. doi:10.1016/j.tiv.2006.10.016.